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University of Arizona · 1 month ago

Clinical Research Coordinator II, Department of Neurology (Full-time) (Multiple) (UPDATED)

Tucson, AZ

Full-time

Onsite

Mid Level

$53K/yr - $66K/yr

3+ years exp

The University of Arizona is seeking a highly motivated Clinical Research Coordinator II to join their Neurology Clinical Research Unit. This role involves coordinating patient enrollment, data management, regulatory compliance, and serving as a liaison among investigators, research staff, and sponsors to advance treatments for neurological diseases.

EducationHigher EducationNon ProfitUniversities

No H1B

Responsibilities

Work with PIs, under moderate guidance, in coordinating activities related to recruitment for clinical trials including recruitment of study participants, conduct interviews, and evaluate potential participants; obtain informed consent, and collect and maintain subject data; perform research subjects’ assessment and Neurologic Rating Scales (NIHSS, mRS, MDS-UPDRS, UDysRS, MoCA, C-SSRS, etc)

Provide input into the design, development, execution and initial interpretation of clinical trial protocols, treatment plans, compliance forms, and tracking documents

Conduct research work and perform professional literature reviews to assist the Principal Investigator in designing appropriate research methodologies, techniques, and procedures

Serve as a patient resource for concerns and information

Prepare, coordinate and/or maintain regulatory documentation including IRB submission and approval of new or revised protocols, safety reports and progress reports

Collect and submit the required documentation to the Institutional Review Board, the University, and corporate or government sponsors. Enter and manage study data in compliance with GCP standards

Participate in data management design and maintenance

Develop administrative and financial recommendations for department management and PIs for research portfolio review. Oversee quarterly review of all Principal Investigator accounts, performing a strategic analysis of PI research portfolios

Collaborate with the Principal Investigator in the preparation of Human Subjects documentation for NIH and other federally funded grant applications

Create and prepare education materials and training to patients, family members, and clinical staff to assure patient safety and adherence to protocols

Administer and assist in the proper collection, processing, storage, and transport of biological specimens and ensure their handling

Order and maintain supplies required for study kits, track spending in this area, and make day-to-day decisions in support of the study

May mentor and train new staff in preparation and conduct of clinical trials

Qualification

Clinical researchIRB processesFDA regulationsGCP guidelinesNeurological disorders knowledgeData managementOrganizational skillsAttention to detailCommunication skillsTeamwork